Could pectin and calcium silicate beat root canal infections?
NCT ID NCT07423663
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase trial tests whether calcium silicate and pectin, placed inside the tooth, can kill bacteria better than standard calcium hydroxide in root canals of dead teeth with abscesses. 63 adults with a single infected premolar will receive one of the three medications. The study measures changes in the types of bacteria present before and after treatment to see which works best.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Calcium silicate, pectin, and calcium hydroxide (as intracanal medications)
- What this could lead to
- If successful, this could point toward better, less resistance-prone disinfectants for root canal treatments.
- What could go wrong
- This is a very early, small trial (63 people) testing only one type of tooth. Results may not apply broadly, and the medications may not outperform standard treatments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
63 people
The number who actually took part.
- Started
-
Sep 2024
- Expected to finish
-
Apr 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
21 to 49 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Patients presenting with a single rooted mandibular premolar tooth with a closed apex and a single patent canal type I in Vertucci's classification (Vertucci et al., 1974). * Having a necrotic pulp. * A pocket depth measurement of \< 3 mm. * Teeth with no previous history of endodontic treatment. * Teeth with periapical lesions of endodontic origin having a periapical index score of 4 or 5 (Orstavik et al., 1986) * Patients who took antibiotics within the period of three months before the study. * Non-restorable teeth. * Teeth with periodontal pockets deeper than 4mm, with or without concomitant or combined endo-perio communication * Multirooted teeth. * Previously initiated or treated teeth. * Teeth with root canal calcifications or resorption. * Teeth with internal/external root resorption or root fracture. * Immune-compromised patients or patients with systemic diseases i.e. (diabetes mellitus, human immunodeficiency virus, leukemia, neutropenia, undergoing chemo- or systemic corticosteroid therapy) * Teeth with root curvature of more than 15 degrees. * Pregnant women * Patients with known sensitivity to the medicaments used in this study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Suez Canal University
Ismailia, Ismailia Governorate, 41511, Egypt
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Other studies related to the condition(s) this trial covers.
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